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Central Monitoring Manager

🕒 6 days ago
Risk-based MonitoringCentralized MonitoringClinical Study Risk ManagementKey Risk Indicators
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📜 Description

  • Lead and facilitate initial and ongoing study risk management.
  • Help select and set up risk-based monitoring platforms.
  • Review Key Risk Indicators, statistical analyses, and Quality Tolerance Limits through centralized monitoring.
  • Present monitoring findings to study teams and clients, and manage issues across functions.
  • Develop study-specific plans and manage targeted SDV, monitoring strategies, and central data review.
  • Contribute risk-based monitoring expertise to proposals and bid defenses, and collaborate on data-driven solutions to study challenges.

🛠️ Requirements

  • College/University degree or an equivalent combination of education, training and experience
  • Clinical study lead/ manager experience
  • Strong communication & presentation skills are essential
  • Leadership and ability to work independently are essential
  • Critical thinking and analytical skills
  • Ability to work with complex data and provide insight into risk reports and trends
  • Ability to adapt to changing circumstances and learn quickly
  • Knowledge of the process and functions in clinical trials, ability to understand the protocol and study associated risks
  • Full working proficiency in English
  • Proficiency in MS Office applications, Excel skills
Full job description

Company Description

PSI is a leading Contract Research Organization with more than 25 years on the market, offering a perfect balance between stability and innovation to both clients and employees.  We focus on delivering quality and on-time services across a variety of therapeutic indications.

    Job Description

    With the industry moving forward, the central monitoring function has become a top priority at PSI. We are looking for a person, who would lead the risk-based monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity.

    You will:

    • Lead and facilitate initial and ongoing study Risk Management
    • Participate in selection and setup of the RBM platform
    • Perform Centralized Monitoring for a study including review of Key Risk Indicators, Statistical Analyses and Quality Tolerance Limits
    • Present Centralized Monitoring analysis results to study teams and clients and manage issues in cross-functional environment
    • Develop and review study-specific Plans
    • Set up and manage targeted SDV and monitoring strategy for a study
    • Set up and manage Central Data Review activities in a study
    • Contribute to Proposals and bid defense meetings with information about Risk Based Monitoring services
    • Communicate study challenges to Clinical Data Science group and work out data-driven solutions
    • Applications must be submitted in English

    Qualifications

    • College/University degree or an equivalent combination of education, training and experience
    • Clinical study lead/ manager experience
    • Strong communication & presentation skills are essential
    • Leadership and ability to work independently are essential
    • Centralized Monitoring experience is a plus
    • Critical thinking and analytical skills
    • Ability to work with complex data and provide insight into risk reports and trends
    • Ability to adapt to changing circumstances and learn quickly
    • Knowledge of the process and functions in clinical trials, ability to understand the protocol and study associated risks
    • Full working proficiency in English
    • Proficiency in MS Office applications, Excel skills

    Additional Information

    This role is not only important for every CRO, but it is booming now. This is an opportunity to work on a frontline of the industry, set the grounds for risk-based models and get a global helicopter view on each project.

    PSI CRO

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    PSI CRO

    Central Monitoring Manager

    🕒 6 days ago
    PSI CRO👥 1001 - 5000 employees🏢 Pharmaceuticals

    Leads risk-based monitoring across clinical studies and programs, overseeing centralized data review, risk analysis, monitoring strategies, and cross-functional communication to support patient safety and data integrity.

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    PSI CRO👥 1001 - 5000 employees🏢 Pharmaceuticals

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